| Weight | 303.156 g/mol |
|---|---|
| Formula | C11H15BrN2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Narcobarbital (125-55-3)
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- Electrolyte concentrations in the blood serum of swine under general anaesthesia produced by administration of chloral hydrate, Nembutal (pentobarbital), Eunarcon (narcobarbital) and Brevinarcon (5-sec-butyl-5-ethyl-2-thiobarbituric acid). (Polskie archiwum weterynaryjne, 1980)
- Debromination and narcobarbital in vitro (Ceskoslovenska farmacie, 1963)
- [Effects of general anaesthesia in pigs, produced by the intravenous administration of chloral hydrate and Eunarcon (narcobarbital), on the acid-base balance in the blood and on the concentration of some electrolytes in the serum.]. (1970)
- Functional state of the liver in swine anaesthetized by intravenous administration of chloral hydrate, Nembutal (pentobarbital), Eunarcon (narcobarbital) and Brevinarcon (5-sec-butyl-5-ethyl-2-thiobarbituric acid). (Polskie archiwum weterynaryjne, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)C1(C(=O)NC(=O)N(C1=O)C)CC(=C)Br
-
InChIKeyWGMASVSHOSNKMF-UHFFFAOYSA-N
- Pubchem - Narcobarbital
- Wikipedia - enibomal
Narcobarbital (Pronarcon) is a barbiturate derivative developed by Riedel de Hean in the 1930s. It is an N-methylated derivative of propallylonal and has similar sedative effects. It is still used in veterinary medicine for inducing surgical anaesthesia.
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